Gilbert Disease [Gilbertova nemoc]
- Terms
-
familiární nehemolytická žloutenka
Gilbertova choroba
Gilbertův syndrom
Gilbertův-Meulengrachtův syndrom
hyperbilirubinemie I
hyperbilirubinémie I
intermitentní hyperbilirubinémie
juvenilní žloutenka
kongenitální nehemolytická žloutenka
kongenitální nonhemolytická žloutenka
Meulengrachtův syndrom
-
Constitutional Liver Dysfunction
Familial Nonhemolytic Jaundice
Gilbert Syndrome
Gilbert-Lereboullet Syndrome
Gilbert's Disease
Gilbert's Syndrome
Hyperbilirubinemia 1
Hyperbilirubinemia I
Hyperbilirubinemia, Arias Type
Meulengracht Syndrome
Unconjugated Benign Bilirubinemia
A benign familial disorder, transmitted as an autosomal dominant trait. It is characterized by low-grade chronic hyperbilirubinemia with considerable daily fluctuations of the bilirubin level.
- DUI
- D005878 MeSH Browser
- CUI
- M0009229
- History note
- 2000(1975)
- Public note
- 2000; see GILBERT'S DISEASE 1991-1999, see HYPERBILIRUBINEMIA, HEREDITARY 1975-90
Allowable subheadings
- BL
- blood 5
- CF
- cerebrospinal fluid 0
- CI
- chemically induced 1
- CL
- classification 0
- CO
- complications 2
- DI
- diagnosis 25
- DG
- diagnostic imaging 0
- DH
- diet therapy 0
- DT
- drug therapy 4
- EC
- economics 0
- EM
- embryology 0
- EN
- enzymology 0
- EP
- epidemiology 2
- EH
- ethnology 0
- ET
- etiology 8
- GE
- genetics 16
- HI
- history 0
- IM
- immunology 0
- ME
- metabolism 4
- MI
- microbiology 0
- MO
- mortality 1
- NU
- nursing 0
- PS
- parasitology 0
- PA
- pathology 3
- PP
- physiopathology 4
- PC
- prevention & control 0
- PX
- psychology 0
- RT
- radiotherapy 0
- RH
- rehabilitation 0
- SU
- surgery 1
- TH
- therapy 3
- UR
- urine 1
- VE
- veterinary 0
- VI
- virology 0